Organic compounds of PM2.5 in Mexico Valley: Spatial and temporal patterns, behavior and sources

• Published in: The Science of the total environment Vol. 409; no. 8; pp. 1453 - 1465
• Main Authors: Amador-Muñoz, O., Villalobos-Pietrini, R., Miranda, J., Vera-Avila, L.E.
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier B.V 15.03.2011; [Amsterdam; New York]: Elsevier Science; Elsevier
• Subjects: Air Pollutants - analysis; Air Pollution - statistics & numerical data; Alkanes - analysis; Applied sciences; Atmosphere - chemistry; Atmospheric pollution; Environmental Monitoring; Exact sciences and technology; Humidity; Mexico; Multivariate analysis; n-Alkanes; Nitro-PAH; Organic Chemicals - analysis; Particle Size; Particulate Matter - analysis; PM2.5; Pollutants physicochemistry study: properties, effects, reactions, transport and distribution; Pollution; Polycyclic aromatic hydrocarbons; Polycyclic Aromatic Hydrocarbons - analysis; Secondary organic aerosol; Temperature; Wind; Central America; Mexico; America; Nitro-PAH; n-Alkanes; Secondary organic aerosol; Polycyclic aromatic hydrocarbons; Multivariate analysis; PM2.5; Nitro compound; Urban area; Mutagen; Spatial variation; Time variation; Persistent organic pollutant; Fine particle; Alkane; Organic compounds; Anthropogenic factor; Natural origin pollution; Factor analysis; Hydrocarbon; Secondary pollutant; Polycyclic aromatic compound; Carcinogen; Biogenic factor; Aerosols; Pollution source inventory; Air pollution; PM; Concentration distribution
• ISSN: 0048-9697; 1879-1026
• DOI: 10.1016/j.scitotenv.2010.11.026

A longitudinal study on spatial and temporal behavior of particles less than 2.5μm (PM2.5), solvent extracted organic matter (SEOM), polycyclic aromatic hydrocarbons (PAH), n-alkanes and nitro-PAH was carried out for a full year in 2006, at five sites simultaneously around the Metropolitan Zone of Mexico Valley (MZMV). There is rather uniform distribution of PM2.5 and SEOM in the MZMV regarding gravimetric mass concentration, while some specific organic chemical components showed mass heterogeneity. The highest mass concentrations of target compounds occurred in the dry seasons with respect to the rainy season. Bonfires and fireworks are probably responsible for extreme values of PM2.5, SEOM and PAH (≥228gmol−1). Benzo[ghi]perylene was the most abundant PAH, with C24–C26 the most abundant n-alkanes and 2-nitrofluoranthene and 9-nitroanthracene the most abundant nitro-PAH. The northeast zone was the area with the greatest presence of sources of incomplete diesel combustion, while the central for gasoline combustion. In the southwest, the biogenic sources were more abundant over the anthropogenic sources. This was opposite to the other sites. Factor analysis allowed us to relate different compounds to emitting sources. Three main factors were associated with combustion, pyrolysis and biogenic primary sources while the other factors were associated with secondary organic aerosol formation and industry. Correlation analyses indicated that SEOM originates from different primary emission sources or is formed by different processes than the other variables, except in southwest. Associations among variables suggest that PM2.5 in the northwest and in the southeast originated mainly from primary emissions or consisted of primary organic compounds. PM2.5 in the northeast, central and southwest contains a greater proportion of secondary organic compounds, with the less oxidized organic aerosols in the northeast and the most aged organic aerosol in the southwest. This follows the trends in the prevailing wind directions in MZMV during 2006. ► We determine specific organic compounds of PM2.5 in Mexico Valley. ► PM2.5, SEOM, biogenic n-alkanes and nitro-PAH are spatially uniform distributed, opposite to PAH. ► Major diesel combustion sources are in NE, Central for gasoline and SW for biogenic. ► PM2.5 in NW and SE were from primary sources; in NE, central and SW is from secondary formation. ► Different sources/formations for SEOM were observed, with secondary photodegradated compounds.